Have questions? Visit https://www.reddit.com/r/SNPedia

rs149753643

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149753643(A;A)
Make rs149753643(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128906208
GeneACAD9
is asnp
is mentioned by
dbSNPrs149753643
ebirs149753643
HLIrs149753643
Exacrs149753643
Varsomers149753643
Maprs149753643
PheGenIrs149753643
hapmaprs149753643
1000 genomesrs149753643
hgdprs149753643
ensemblrs149753643
gopubmedrs149753643
geneviewrs149753643
scholarrs149753643
googlers149753643
pharmgkbrs149753643
gwascentralrs149753643
openSNPrs149753643
23andMers149753643
23andMe allrs149753643
SNP Nexus

SNPshotrs149753643
SNPdbers149753643
MSV3drs149753643
GWAS Ctlgrs149753643
Max Magnitude0
ClinVar
Risk rs149753643(A;A)
Alt rs149753643(A;A)
Reference rs149753643(G;G)
Significance Pathogenic
Disease Acyl-CoA dehydrogenase family
Variation info
Gene ACAD9
CLNDBN Acyl-CoA dehydrogenase family, member 9, deficiency of
Reversed 0
HGVS NC_000003.11:g.128625051G>A
CLNSRC
CLNACC RCV000201643.1,